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  • Handbook of Pharmaceutical Wet Granulation: Theory and Practice in a Quality by Design Paradigm

    Handbook of Pharmaceutical Wet Granulation by Narang, Ajit S.; Badawy, Sherif I.F.;

    Theory and Practice in a Quality by Design Paradigm

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      • Publisher's listprice EUR 197.00
      • The price is estimated because at the time of ordering we do not know what conversion rates will apply to HUF / product currency when the book arrives. In case HUF is weaker, the price increases slightly, in case HUF is stronger, the price goes lower slightly.

        81 705 Ft (77 815 Ft + 5% VAT)
      • Discount 10% (cc. 8 171 Ft off)
      • Discounted price 73 535 Ft (70 034 Ft + 5% VAT)

    81 705 Ft

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    printed on demand

    Why don't you give exact delivery time?

    Delivery time is estimated on our previous experiences. We give estimations only, because we order from outside Hungary, and the delivery time mainly depends on how quickly the publisher supplies the book. Faster or slower deliveries both happen, but we do our best to supply as quickly as possible.

    Product details:

    • Publisher Elsevier Science
    • Date of Publication 4 December 2018

    • ISBN 9780128104606
    • Binding Hardback
    • No. of pages890 pages
    • Size 234x190 mm
    • Weight 2040 g
    • Language English
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    Long description:

    Handbook of Pharmaceutical Wet Granulation: Theory and Practice in a Quality by Design Paradigm offers a single and comprehensive reference dedicated to all aspects of pharmaceutical wet granulation, taking a holistic approach by combining introductory principles with practical solutions. Chapters are written by international experts across industry, academic and regulatory settings, and cover a wide spectrum of relevant and contemporary wet granulation topics, techniques and processes. The books' focus on process analytical technology, quality by design principles, granulation equipment, modeling, scale-up, control and real time release makes it a timely and valuable resource for all those involved in pharmaceutical wet granulation.

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    Table of Contents:

    Section I: Physicochemical Principles and Fundamentals of Wet Granulation
    Section II: Critical Quality Attributes of Drug Products and Process Design Solutions
    Section III:ï¿1⁄2 Process-Stability Interactions and Optimization
    Section IV:ï¿1⁄2 Material Attributes Critical to Wet Granulation Process Performance
    Section V: Process Modeling
    Section VI: Scale-up
    Section VII:ï¿1⁄2 Process Development and Process Analytical Technology Applications
    Section VIII:ï¿1⁄2 Real-Time Release, Real-time Release Testing, and Drug Product Control Strategy Development

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